chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	47286922	47286923	A	C	27	GENIC	possibly homozygous	109381795
20	47289123	47289124	A	T	9	GENIC	homozygous	109212398
20	47289141	47289142	A	T	12	GENIC	homozygous	109212400
20	47295260	47295261	T	C	16	GENIC	homozygous	109381824
20	47291692	47291693	C	T	11	GENIC	homozygous	109513752
20	47295832	47295833	G	A	18	GENIC	homozygous	109513754
20	47297660	47297661	G	T	25	GENIC	homozygous	109513756
20	47298935	47298936	C	G	25	GENIC	homozygous	109276484
20	47302051	47302052	G	A	6	GENIC	homozygous	109381873
20	47302500	47302501	C	G	12	GENIC	homozygous	109381876
20	47302552	47302553	G	T	7	GENIC	homozygous	109513758
20	47303685	47303686	C	T	25	GENIC	possibly homozygous	109404986
20	47304267	47304268	T	C	5	GENIC	homozygous	109513760
20	47304300	47304301	A	G	8	GENIC	homozygous	109381878
20	47304361	47304362	C	T	8	GENIC	homozygous	109513762
20	47304459	47304460	T	C	16	GENIC	homozygous	109404987
20	47304577	47304578	T	C	12	GENIC	homozygous	109513764
20	47305515	47305516	T	C	9	GENIC	homozygous	109381880